# Mindchild Medical

- Location (FDA's records): North Andover, MA
- FDA decisions: 3 (2012–2017): 3 510(k) clearances
- Product codes: HGM (3)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Monica Healthcare, Ltd.: 1 (https://510kreport.com/company/monica-healthcare)
- Hewlett-Packard Co.: 1 (https://510kreport.com/company/hewlett-packard)

## Its most-cited devices
- K120018: Mindchild Meridian Fetal Heart Rate Monitor (2012), cited by 1

## Recent decisions
- K161902: Meridian M110 Fetal Monitoring System (Jan 12, 2017)
- K142883: MindChild Meridian M100 Fetal Heart Rate Monitor (Apr 17, 2015)
- K120018: Mindchild Meridian Fetal Heart Rate Monitor (Sep 19, 2012)

Source page: https://510kreport.com/company/mindchild-medical